FDA applicant
Baisheng Medical Co., Ltd.
FDA records 5 decisions for Baisheng Medical Co., Ltd. (Jiangmen, CN) from 2017 to 2025: 5 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and GXY (Electrode, Cutaneous). Since 2016 its 510(k)s took a median of 146 days from receipt to decision, against 125 for FDA’s reviews in the same codes and years. Its devices cite 3 predicates, 1 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Baisheng Medical Co., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
2in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2017.
Planning a device like Baisheng Medical Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report